drugset / Trial / NCT00873561
A Study to Evaluate NBI-6024 in Adult and Adolescent Patients With New Onset of Type 1 Diabetes Mellitus
RandomizedParallel-groupDouble-blindBasic science
Summary
This was a study designed to evaluate the efficacy of multiple doses of an investigational drug, NBI-6024, in adult (18 to 35 years of age) and adolescent (10 to 17 years of age) patients with new onset type 1 diabetes mellitus, on endogenous insulin production. A total of 188 patients were enrolled in the study. The study was divided into three periods: screening, treatment (comprising an induction phase and maintenance phase), and follow-up. NBI-6024 was generally well tolerated and exhibits a benign safety profile, as there were no significant safety issues with NBI-6024 treatment. In summary, NBI-6024 did not demonstrate statistically significant efficacy compared with placebo.
Timeline
- Start
- 2001-12
- Primary completion
- 2006-04
- Completion
- 2006-07
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Comparator | NBI-6024 | Peptide | 0.1 mg | Subcutaneous |
| Comparator | NBI-6024 | Peptide | 0.5 mg | Subcutaneous |
| Comparator | NBI-6024 | Peptide | 1 mg | Subcutaneous |